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Internship Cqe Jobs (NOW HIRING)

Howmet

Quality Engineer - Plant 10

Whitehall, MI · On-site

$68K - $88K/yr

Experience working in an internship or co-op capacity in a manufacturing or lab environment * 3 ... ASQ, CQA, and/or CQE preferred * Experience in aerospace or automotive * Excellent PC skills ...

Howmet

Quality Engineer - Plant 3

Whitehall, MI · On-site

$68K - $88K/yr

Experience working in an internship or co-op capacity in a manufacturing or lab environment * 3 ... ASQ, CQA, and/or CQE preferred * Experience in aerospace or automotive * Excellent PC skills ...

Micron

Senior Product Quality Engineer

Boise, ID

Internship or project experience in semiconductor or electronics industries * Experience with yield ... ASQ CQE or similar quality certification As a world leader in the semiconductor industry, Micron is ...

Danaher

Quality Operations Engineer

Lodi, CA · On-site

$70K - $85K/yr

... internship/co-op experience may be considered) * Foundational understanding of quality concepts and ... Examples may include but are not limited to the CQE, CRE, CQA, etc. Cepheid, a Danaher operating ...

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How much do internship cqe jobs pay per hour?

As of Jul 13, 2026, the average hourly pay for internship cqe in the United States is $16.65, according to ZipRecruiter salary data. Most workers in this role earn between $14.42 and $18.51 per hour, depending on experience, location, and employer.

What is the difference between Internship Cqe vs Quality Assurance Tester?

AspectInternship CqeQuality Assurance Tester
Required CredentialsTypically pursuing or recent graduate in related fieldHigh school diploma or equivalent; some roles prefer certifications
Work EnvironmentInternship setting, learning-focused, entry-levelFull-time or part-time, testing software in office or remote
Employer & Industry UsageInternships offered by tech companies, software firms, or QA departmentsUsed across software, gaming, and app development industries

Internship Cqe is an entry-level, learning-focused position often held by students or recent graduates, providing hands-on experience in quality control processes. In contrast, a Quality Assurance Tester is a more experienced role responsible for testing software products to identify bugs and ensure quality. While both roles involve quality assessment, internships are designed for skill development, whereas QA testers perform ongoing testing tasks within professional teams.

What are the key skills and qualifications needed to thrive as a CQE (Customer Quality Engineer) Intern, and why are they important?

To thrive as a CQE Intern, you need a solid foundation in engineering principles, quality control concepts, and data analysis, typically supported by progress toward a degree in engineering or a related field. Familiarity with quality management systems (such as ISO 9001), statistical analysis tools, and software like Microsoft Excel or Minitab is often required. Strong problem-solving ability, attention to detail, and effective communication skills help interns excel in cross-functional teams and manage customer quality concerns. These skills are crucial for identifying and resolving quality issues, ensuring customer satisfaction, and supporting continuous improvement efforts.

What types of projects or tasks can I expect to work on during a CQE internship?

As a CQE (Customer Quality Engineer) intern, you will typically support the quality engineering team by assisting with data analysis, root cause investigations, and process improvement initiatives. Common tasks include preparing quality reports, participating in failure analysis, and helping implement corrective actions. You may also collaborate with cross-functional teams such as manufacturing, engineering, and customer support to address product quality concerns. This hands-on experience provides valuable insight into quality management systems and the real-world application of engineering principles.

What are Internship CQE positions?

Internship CQE positions are internship roles focused on Customer Quality Engineering (CQE). These internships provide students or entry-level professionals with hands-on experience in quality assurance processes, root cause analysis, and problem-solving related to customer-reported issues in manufacturing or tech environments. Interns typically assist CQE teams in monitoring production quality, handling customer feedback, and helping to implement corrective actions. These roles are ideal for those studying engineering, quality management, or related fields and seeking practical experience in quality engineering within a customer-oriented framework.
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Internship Cqe jobs near you
Infographic showing various Internship Cqe job openings in the United States as of July 2026, with employment types broken down into 76% Internship, 12% As Needed, and 12% Full Time. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $34,624 per year, or $16.6 per hour.
Sr. Quality Engineer, Quality Operations - Wayne, NJ

Sr. Quality Engineer, Quality Operations - Wayne, NJ

Getinge

Wayne, NJ • On-site

$115K - $120K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 5 days ago

Getinge rating

9.3

Company rating: 9.3 out of 10

Based on 14 frontline employees who took The Breakroom Quiz

9th of 430 rated machine equipment manufacturers

Job description

With a passion for life
Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers - and to save more lives, we need team players, forward thinkers, and game changers.
Are you looking for an inspiring career? You just found it.
Job Overview
As a Sr. Quality Engineer specializing in Quality Operations, you will be responsible for overseeing and improving the quality of manufacturing processes, ensuring compliance with regulatory requirements, and driving continuous improvement initiatives to enhance product quality and customer satisfaction. You will play a key role in ensuring that our manufacturing operations meet the highest standards of quality and efficiency while adhering to relevant regulations and industry best practices.
Job Responsibilities and Essential Duties
  • Develop, implement, and maintain quality control processes and procedures for manufacturing operations to ensure compliance with regulatory requirements and industry standards.
  • Establish and monitor key performance indicators (KPIs) to assess manufacturing quality and identify opportunities for improvement.
  • Participate/ Lead validation and verification activities for manufacturing processes, equipment, and software systems to ensure they meet quality and regulatory requirements.
  • Develop/ review validation protocols, execute validation studies, and analyze data to ensure process robustness and reliability.
  • Ensures through Design Transfer activities the Device Master Records (DMRs) contents are developed, controlled, and maintained leading to Risk based Manufacturing Control Plans.
  • Support/ Investigate and resolve Out of Tolerance events identified during equipment/ instrument calibrations.
  • Investigate product nonconformances, conduct root cause analysis, and implement corrective and preventive actions (CAPA).
  • Track and monitor CAPA effectiveness to ensure issues are resolved and prevented.
  • Support the Health and Hazard Evaluation process by gathering required data and performing in-depth analysis prior to sharing the information with the Field Action Committee.
  • Implement corrective and preventive actions (CAPAs) to address root causes and prevent recurrence of quality issues.
  • Facilitate risk management activities related to manufacturing processes, identifying, and mitigating risks to product quality, safety, and efficacy.
  • Implement risk-based decision-making processes to prioritize quality activities and allocate resources effectively.
  • Lead and support continuous improvement projects aimed at enhancing manufacturing processes, reducing defects, and optimizing productivity.
  • Utilize quality tools and methodologies, such as Six Sigma, Lean Manufacturing, and Statistical Process Control (SPC), to drive process optimization and waste reduction.
  • Ensure compliance with applicable regulations, including FDA Quality System Regulation (QSR), ISO 13485, and other international standards.
  • Support both internal and external audits as an SME for Production & Process Controls and presents records of activities related to Design Transfer for New Product Development and Design Changes.
  • Provide mentorship and guidance to new Engineers/Interns within the organization.

Minimum Requirements
  • Bachelor's degree in engineering, Science, or other related field is required. ASQ, CQE, Six Sigma Green Belt or other applicable certifications are a plus.
  • A minimum of 7 years' experience in Quality or Engineering.
  • Experience in a medical device or pharmaceutical industry.
  • Experience with Class III disposable and/or Electro-Mechanical medical devices is preferred.
  • Knowledge and understanding of the US Food and Drug Administration (FDA) 21 CFR 820, ISO 13485, ISO 14971, EU MDD, and EU MDR. Knowledgeable on specific requirements for Design Controls and Risk Management is preferred.

Required Knowledge, Skills, and Abilities
  • Knowledge of application & selection of Sampling Plans, to support Risk based Manufacturing Controls Plans.
  • Project management and leadership experience is desirable.
  • Strong analytical and problem-solving skills.
  • Excellent communication and interpersonal skills.
  • Proficiency in quality tools and methodologies (e.g., Six Sigma, FMEA, Gage R&R).
  • Ability to work effectively in a cross-functional team environment.
  • Ability to review and understand technical standards and their requirements for products.
  • Proficiency in Microsoft Office Products such as Word, Excel, or equivalent software applications.

Salary range: $115k - $120k plus 10% annual bonus
#LI-LG1
About us
With a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the products are sold in more than 135 countries.
Benefits at Getinge:
At Getinge, we offer a comprehensive benefits package, which includes:
  • Health, Dental, and Vision insurance benefits
  • 401k plan with company match
  • Paid Time Off
  • Wellness initiative & Health Assistance Resources
  • Life Insurance
  • Short and Long Term Disability Benefits
  • Health and Dependent Care Flexible Spending Accounts
  • Commuter Benefits
  • Parental and Caregiver Leave
  • Tuition Reimbursement

Getinge is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, pregnancy, genetic information, national origin, disability, protected veteran status or any other characteristic protected by law. Reasonable accommodations are available upon request for candidates taking part in all aspects of the selection process.

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About Getinge

Sourced by ZipRecruiter

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Dr Wayne, NJ, US

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